Our client is one of the biggest global medical producers and a very influential pharmaceutical supplier in the Netherlands. The company specialises in developing biological therapies and medicine to cure oncology, hematology, kidney, bone, and cardiovascular diseases. Are you ready to contribute to their mission of serving patients with the highest quality?
You will take responsibility of providing guidance and being the first point of contact of the Production staff, navigating how to effectively comply with SOPs and GMP. Moreover, your daily tasks will focus on reviewing the assembled, packaged, and labelled batches. Working in shifts you will be performing QA operations and supporting the manufacturing area.
-Performing production checks and GMP compliance checks;
-Checking and approving deviation records as well as initiating and owning QA deviations when needed;
-Taking ownership of operational SOP's and performing SOP's inspections;
-Developing and holding the GMP trainings for QA and manufacturing staff;
-Preparing weekly and monthly metrics as well as taking ownership of the departmental performance boards.
-Master's degree in Pharmacy or a related Life Sciences field;
-Around 3 years of QA or manufacturing experience working with medical devices or in a pharmaceutical industry;
-Experience in batch record review and quality investigations;
-Knowledge of GMP, GDP, GCP and understanding of their practical application.
Please note! In this job you will be working in 3 shifts: Early shift: 6:30-15:00, Late shift: 14:30 - 23:00, Night shift: 22:30 - 7:00.
Are you interested in this or another role? Do not hesitate to contact me at email@example.com or by applying to this position.